Variant report

Variant	rs56395966
Chromosome Location	chr13:51617687-51617688
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51614600-51618200	Enhancers	Fetal Brain Male	brain
2	chr13:51614600-51619400	Enhancers	Fetal Brain Female	brain
3	chr13:51615000-51618200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr13:51617200-51617800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr13:51617200-51618000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:51617200-51620000	Enhancers	Brain Germinal Matrix	brain
7	chr13:51617400-51617800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:51617400-51618000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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